Pyridine 3 Bromo 2 Bromomethyl
pyridine pyrrole pyrazine piperidine piperazine

pyridine, 3-bromo-2-(bromomethyl)-

    Specifications

    HS Code

    193829

    Chemical Formula C6H5Br2N
    Molar Mass 250.92 g/mol
    Appearance Solid (usually)
    Melting Point Data may vary, needs experimental determination
    Boiling Point Data may vary, needs experimental determination
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in many organic solvents like dichloromethane, chloroform
    Density Data may vary, needs experimental determination
    Flash Point Data may vary, needs experimental determination
    Hazard Class Harmful, may cause irritation to skin, eyes and respiratory system

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    General Information
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    Frequently Asked Questions

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    What are the physical properties of 3-bromo-2- (bromomethyl) pyridine?
    3-Mercury-2- (mercury methyl) alkyl is a class of organic compounds containing mercury. Mercury, known as "mercury", is liquid at room temperature and has a metallic luster. In such compounds, mercury atoms are connected to methyl and alkyl groups, giving them unique physical and chemical properties.
    In terms of physical properties, 3-mercury-2- (mercury methyl) alkyl compounds are usually liquid or low-melting solid at room temperature and pressure. Due to the large relative atomic mass of mercury atoms, their density is high. And the volatility of such compounds is lower than that of ordinary organic compounds. However, due to the volatility of mercury itself, some mercury-containing organic compounds will also evaporate into the air.
    Its solubility is also unique. In organic solvents such as benzene and ether, the compound has a certain solubility, but its solubility in water is extremely low. This is because the molecular structure of the compound is dominated by organic groups and has strong hydrophobicity.
    From a chemical point of view, the stability of mercury-carbon bonds in 3-mercury-2- (mercury methyl) alkyl compounds is limited. Under certain chemical reaction conditions, such as high temperature, strong acid or specific catalysts, the mercury-carbon bond is prone to fracture, and then mercury ions or small molecules containing mercury are released. Mercury ions are very toxic and extremely harmful to organisms. At the same time, the alkyl group in such compounds can participate in some common organic reactions, such as substitution reactions, oxidation reactions, etc. However, due to the presence of mercury atoms, the reaction activity and selectivity will be affected. Moreover, such compounds are also less stable in the environment and are easily decomposed by light and microorganisms. Their decomposition products may further participate in various chemical and biological cycles in the environment, which may have a potential impact on the ecological environment.
    What are the chemical properties of 3-bromo-2- (bromomethyl) pyridine?
    3-Hydroxy- 2 - (hydroxymethyl) pyridine, this substance has many chemical properties. It is basic, because the nitrogen atom of the pyridine ring has lone pairs of electrons, and can accept protons. In acidic solutions, it can combine with protons to form pyridine cations, and this alkalinity makes it a base catalyst. In some organic reactions, it can assist in the conversion of reactants.
    Furthermore, it is nucleophilic. The oxygen atoms of hydroxyl groups and hydroxymethyl groups are rich in electrons and are easy to attack electrophilic reagents. For example, when encountering halogenated hydrocarbons, hydroxyl oxygen atoms can use nucleophilic substitution reactions to form ether compounds; the oxygen atoms of hydroxymethyl groups can also do the same, participating in the construction of more complex molecular structures.
    In addition, it is reducing. Hydroxyl groups can be oxidized, and can be converted into aldehyde groups, carboxyl groups, etc. under the action of appropriate oxidizing agents. In case of mild oxidizing agents, hydroxyl groups may be oxidized to aldehyde groups to form compounds containing aldehyde groups and pyridine rings; if the oxidizing agent is strong, aldehyde groups may be further oxidized to carboxyl groups.
    At the same time, the pyridine ring makes it stable and aromatic. The pyridine ring conforms to the Shocker rule and has an aromatic conjugate system, which endows the substance with certain chemical stability. Under some reaction conditions, the structure of the pyridine ring can be maintained stable, providing a stable framework for the reaction, which is convenient for other groups to undergo various reactions on it to synthesize various pyridine derivatives.
    What is the synthesis method of 3-bromo-2- (bromomethyl) pyridine?
    To prepare 3-hydroxy- 2 - (hydroxymethyl) pyridine, the method of synthesis has been explored by chemists throughout the ages, and many paths have been obtained. One of them is described in detail below.
    Pyridine can be used as the starting material. First, pyridine and formaldehyde are reacted at a suitable temperature in the presence of a specific basic catalyst. This reaction condition is quite critical, and the temperature needs to be finely regulated, about a certain range (such as X ° C - Y ° C). The amount of basic catalyst also needs to be precisely controlled to ensure that the reaction proceeds in the desired direction. The nitrogen atom of pyridine has unique electronic properties, and in an alkaline environment, it can undergo nucleophilic addition reaction with the carbonyl group of formaldehyde to form a preliminary product. In this preliminary product, hydroxymethyl groups are introduced at specific positions in the pyridine ring.
    Then, the resulting product is further oxidized. Select a suitable oxidizing agent, such as a certain type of metal oxide or a specific organic oxidizing agent, and carry out the oxidation process under specific reaction media and conditions. This oxidation step aims to convert the hydrogen atom at another position on the pyridine ring into a hydroxyl group, so as to achieve the synthesis of the target product 3-hydroxy- 2- (hydroxymethyl) pyridine.
    The whole synthesis process is like a craftsman's carving utensil, and each step needs to be carefully done. The purity of the raw material and the control of the reaction conditions are all related to the yield and purity of the product. If there is a slight error, it may deviate from the expected path, produce impurities, or greatly reduce the yield. Only by carefully studying all aspects and following the scientific method can 3-hydroxy- 2 - (hydroxymethyl) pyridine be successfully prepared.
    What are the main uses of 3-bromo-2- (bromomethyl) pyridine?
    3-2- (methyl) pyridine, which is an important chemical compound, has its main use.
    First, it is large in the field of chemical production. It can be used in the synthesis of chemical compounds, and is used for many chemical compounds with special effects. Such as the synthesis of some antibacterial compounds, 3-2- (methyl) pyridine. Among them, its special properties can make the synthetic chemical more effective, which can effectively inhibit the growth and reproduction of specific bacteria, and can be used for the purpose of treating diseases and saving people.
    Second, it also has extraordinary performance in the field of materials. It can be used as a synthetic raw material for functional materials. From a specific chemical reaction, its introduction into polymer materials can improve the properties of the material. For example, the qualitative and anti-corrosion properties of the material can be improved. In this way, the obtained materials can be used in aerospace, electronics and other high-end fields to improve the performance of phase products.
    Third, it is also indispensable in the chemical and catalytic field. Because its molecules contain specific active groups, it can be used as a catalyst or a part of catalysis. In some synthetic reactions, it can effectively reduce the activation energy of the reaction, accelerate the reaction rate, improve the reaction performance, and make the reaction more efficient and precise. It has an important role in the development of chemical engineering.
    Therefore, 3 - 2 - (methyl) pyridine plays an important role in the field of chemistry, materials, catalysis, etc., and there are many steps to be taken in this field.
    What are the precautions for the storage and transportation of 3-bromo-2- (bromomethyl) pyridine?
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    In the case of tricyanobis (cyanomethyl) alkyne, many precautions need to be paid attention to during storage and transportation.
    The first to bear the brunt, this material has considerable chemical activity, and must be stored in a cool, dry and well-ventilated place. If it is in a humid or high temperature environment, it may cause chemical reactions, cause material deterioration, or even be dangerous. The humid gas is easy to react with its components, and high temperature can promote the reaction to accelerate, which is not a good situation.
    Furthermore, its storage should be kept away from fire and heat sources. When these substances encounter open flames and hot topics, it is very likely to cause combustion or even explosion. Therefore, fireworks are strictly prohibited around, and electrical equipment must also meet explosion-proof standards to prevent small sparks from causing major disasters.
    When transporting, the packaging must be solid and reliable. Appropriate packaging materials need to be selected to ensure that the substance does not leak in the case of bumps, vibrations, etc. And the packaging should be clearly marked with warning signs, so that both the carrier and the transporter can understand its danger and treat it with caution.
    And because of its special chemical properties, during transportation, it is not allowed to mix with oxidizing substances, acids, alkalis, etc. These substances can easily trigger violent chemical reactions and endanger transportation safety.
    In addition, those involved in storage and transportation must undergo professional training and be familiar with the characteristics of the substance and emergency treatment methods. In the event of leakage and other emergencies, it can be disposed of quickly and properly to minimize the harm. In this way, the safety of cyanobi- (cyanomethyl) alkyne in storage and transportation can be obtained.